Canonical Allele Identifier: CA471214151
Gene: LINC01475 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.101287694A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99527937A>G , CM000672.2:g.99527937A>G GRCh38
NC_000010.10:g.101287694A>G , CM000672.1:g.101287694A>G GRCh37
NC_000010.9:g.101277684A>G NCBI36
NG_016854.1:g.5A>G

Transcript Alleles

HGVS Amino-acid change
NR_120618.1:n.446T>C